Development, Characterization, and Immunomodulatory Evaluation of Carvacrol-loaded Nanoemulsion

被引:28
作者
Barros Dantas, Amanda Gabrielle [1 ]
de Souza, Rafael Limongi [1 ]
de Almeida, Anderson Rodrigues [2 ]
Xavier Junior, Francisco Humberto [3 ]
da Rocha Pitta, Maira Galdino [2 ]
Barreto de Melo Rego, Moacyr Jesus [2 ]
Oliveira, Elquio Eleamen [1 ]
机构
[1] State Univ Paraiba, Lab Synth & Drug Delivery, BR-58071160 Joao Pessoa, Paraiba, Brazil
[2] Univ Fed Pernambuco, Lab Immunomodulat & Novel Therapeut Approaches, BR-50670901 Recife, PE, Brazil
[3] Univ Fed Paraiba, Dept Pharm Fed, BR-58051900 Joao Pessoa, Paraiba, Brazil
关键词
carvacrol; cytokine; immunoregulation; nanoemulsion; ANTIMICROBIAL ACTIVITY; INFLAMMATORY RESPONSE; DELIVERY-SYSTEMS; OIL; ANTIOXIDANT; STABILITY; EMULSIONS; CYTOKINES;
D O I
10.3390/molecules26133899
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carvacrol (CV) is an essential oil with numerous therapeutic properties, including immunomodulatory activity. However, this effect has not been studied in nanoemulsion systems. The objective of this study was to develop an innovative carvacrol-loaded nanoemulsion (CVNE) for immunomodulatory action. The developed CVNE comprised of 5% w/w oily phase (medium chain triglycerides + CV), 2% w/w surfactants (Tween 80(R)/Span 80(R)), and 93% w/w water, and was produced by ultrasonication. Dynamic light scattering over 90 days was used to characterize CVNE. Cytotoxic activity and quantification of cytokines were evaluated in peripheral blood mononuclear cell (PBMC) culture supernatants. CVNE achieved a drug loading of 4.29 mg/mL, droplet size of 165.70 +/- 0.46 nm, polydispersity index of 0.14 +/- 0.03, zeta potential of -10.25 +/- 0.52 mV, and good stability for 90 days. CVNE showed no cytotoxicity at concentrations up to 200 mu M in PBMCs. CV diminished the production of IL-2 in the PBMC supernatant. However, CVNE reduced the levels of the pro-inflammatory cytokines IL-2, IL-17, and IFN-gamma at 50 mu M. In conclusion, a stable CVNE was produced, which improved the CV immunomodulatory activity in PBMCs.
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页数:11
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